Gas-Trak 2 Synthetic Blood Gas Control

FDA 510(k) K820705 · United Diagnostics, Inc.

Substantially Equivalent

510(k) numberK820705

Submission

Device name
Gas-Trak 2 Synthetic Blood Gas Control
Applicant
United Diagnostics, Inc.
Mchenry, IL, US
Received
March 16, 1982
Decision date
April 1, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJS – Controls For Blood-Gases, (Assayed And Unassayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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K022529Liquichek Blood Gas Plus Co-Oximeter Control (Il Synthesis Series) Levels 1,2, and 3…JJS · Traditional Bio-Rad08/15/2002SE
K022525Liquichek Blood Gas Plus Co-Oximeter Control (Radiometer 700 Series) Levels, 1,2 and 3…JJS · Traditional Bio-Rad08/15/2002SE
K003242Liquichek Blood Gas Plus Co-Oximeter Control (Il), Model 621,622,623JJS · Traditional Bio-Rad11/30/2000SE
K003239Liquichek Blood Gas Plus Co-Oximeter Control (800 Series), MODEL504,505,506JJS · Traditional Bio-Rad11/30/2000SE
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More from Bio-Rad

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K884977Gas Trak PlusJJY · Traditional 01/27/1989SE
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K843986Stat-Trak Plus Liquid Chemistry Controls 1,2 & 3JJY · Traditional 11/27/1984SE
K831389Stat-Trak Liquid Electrolyte ControlJJR · Traditional 08/10/1983SE
K831814Calibration Standard-HemoglobinKRZ · Traditional 07/28/1983SE
K831813Co-Oximeter ControlKHG · Traditional 07/28/1983SE
K831075Blood Gas & Flame Photometer Instru-CGC · Traditional 06/22/1983SE
K813517Blood Gas Analysis, Standards ControlsCHL · Traditional 12/31/1981SE
K810618Ampuled Flame Photometer StandardsJIS · Traditional 03/31/1981SE

Questions and answers

When was Gas-Trak 2 Synthetic Blood Gas Control cleared by the FDA?

Gas-Trak 2 Synthetic Blood Gas Control (K820705) received a 510(k) decision of Substantially Equivalent on April 1, 1982, 16 days after the submission was received.

What is the product code of K820705?

The FDA product code is JJS – Controls For Blood-Gases, (Assayed And Unassayed), a Class I (low risk) device regulated under 21 CFR 862.1660.